B

Baxter International

Global provider of medical care products

Manager Regulatory Affairs

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeDeerfield, IL, USA

About the Job

Requirements

  • A bachelor's degree in a scientific discipline or equivalent.
  • At least 5 years of Regulatory Affairs experience or related experience within a regulated industry.
  • Experience leading projects, cross-functional initiatives, and/or people-management responsibilities.
  • Knowledge of global regulatory requirements, guidance documents, and compliance expectations.
  • A strong understanding of product lifecycle management and regulatory submission processes.
  • Demonstrated ability to assess regulatory risks and develop effective mitigation strategies.
  • Strong communication, presentation, and stakeholder-management skills.
  • Ability to manage multiple priorities and deliver results in a fast-paced environment.
  • Experience collaborating effectively within cross-functional and global teams.
  • Experience working directly with global health authorities and regulatory agencies.
  • Experience supporting complex product-development programs and marketed product portfolios.
  • Demonstrated success leading regulatory strategy for global submissions and approvals.
  • Experience representing Regulatory Affairs in industry organizations, trade associations, or external working groups.
  • Prior people-management experience with responsibility for coaching and developing team members.
  • Experience working in multinational and multicultural business environments.
  • Applicants must be authorized to work for any employer in the United States.

Responsibilities

  • Develop and execute regulatory strategies aligned with business objectives for new product development and lifecycle management activities.
  • Lead regulatory activities for assigned product portfolios, ensuring timely submissions, approvals, and compliance commitments.
  • Identify regulatory risks, assess potential impacts, and implement mitigation strategies to support project success.
  • Monitor global regulatory requirements and ensure compliance with applicable regulations, standards, and Baxter procedures.
  • Conduct regulatory gap assessments and implement process improvements to enhance compliance and operational efficiency.
  • Develop, document, and defend regulatory positions and recommendations based on sound regulatory and scientific principles.
  • Serve as the primary regulatory contact with health authorities and support regulatory communications and interactions.
  • Partner with cross-functional teams to align regulatory strategies, timelines, and deliverables with business objectives.
  • Provide strategic regulatory guidance throughout product development and lifecycle management activities.
  • Review and contribute to regulatory-related procedures and documentation to ensure alignment with evolving global requirements.
  • Represent Baxter in industry associations, trade organizations, and external working groups as appropriate.
  • Lead, coach, and develop regulatory team members while fostering a collaborative and high-performing environment.

About the Company

Baxter International

Global provider of medical care products

Baxter International develops and manufactures medical products and equipment for hospitals and blood banks. Its products include sterile IV solutions and blood storage containers; innovations like the Transfuso-Vac extended blood shelf life, and a plastic blood bag helped shape modern blood banking. The company differs from competitors through a long track record of sterile manufacturing, blood-storage innovations, and strategic mergers that broaden its product portfolio. Its goal is to provide reliable, safe medical products that support patient care and hospital operations worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Deerfield, IL
Founded
1931

Recently Posted Jobs

Explore more opportunities at Baxter International

See more jobs